Capobianchi M R, Facchini J, Di Marco P, Antonelli G, Dianzani F
Proc Soc Exp Biol Med. 1985 Apr;178(4):551-6. doi: 10.3181/00379727-178-42041.
Cells infected with viruses and fixed when viral antigens appeared at the cell membrane induced much higher alpha interferon (IFN-alpha) levels in human peripheral blood mononuclear cells (PBMC) than free virions. Relatively few inducer cells were sufficient for triggering IFN production. Optimal IFN yields depended on inducer/producer cell ratio. The response was peculiar to PBMC as it was not found in other cells in which IFN can normally be induced by free virions. IFN inducing activity was also exerted by live virus-infected PBMC, showing that this type of induction may have physiological importance. These findings confirm that viral induction of IFN-alpha is activated by some interaction between viral components presented at the cell surface and PBMC membrane. Thus induction of IFN by circulating cells infected by viruses and presenting viral antigens at the surface may be an efficient host defense mechanism. Since IFN yields close to 10(6) international units per milliliter are obtained, this system has potential for large scale production of native IFN-alpha.
当病毒抗原出现在细胞膜上时被感染并固定的细胞,在人外周血单核细胞(PBMC)中诱导产生的α干扰素(IFN-α)水平比游离病毒粒子高得多。相对较少的诱导细胞就足以触发IFN的产生。最佳的IFN产量取决于诱导细胞/产生细胞的比例。这种反应是PBMC所特有的,因为在其他通常可被游离病毒粒子诱导产生IFN的细胞中未发现这种反应。活病毒感染的PBMC也具有IFN诱导活性,表明这种诱导类型可能具有生理重要性。这些发现证实,IFN-α的病毒诱导是由细胞表面呈现的病毒成分与PBMC膜之间的某种相互作用激活的。因此,被病毒感染并在表面呈现病毒抗原的循环细胞诱导产生IFN可能是一种有效的宿主防御机制。由于每毫升可获得接近10^6国际单位的IFN产量,该系统具有大规模生产天然IFN-α的潜力。